Leads drug discovery programs from target identification to preclinical candidate nomination. Designs and directs medicinal chemistry and biology research programs. Provides scientific leadership and mentors senior scientists in research teams. Represents science function at internal portfolio review and governance committees. Manages relationships with academic collaborators and external research partners. Develops research strategies and prioritizes drug discovery projects. Reviews and approves scientific reports, study designs, and publications. Supports drug candidate selection and IND filing with scientific data. Leads intellectual property strategy including patent filings and FTO analysis. Publishes scientific papers and presents research at international conferences. Manages discovery department budget and scientific resource allocation. Supports BD&L activities through target and compound evaluation activities. Stays current with disease biology, novel target classes, and drug discovery innovation.

Executes validation and qualification activities for pharmaceutical manufacturing equipment. Prepares Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Conducts cleaning validation and prepares cleaning validation protocols and reports. Performs process validation including prospective, concurrent, and retrospective validation. Manages computer system validation (CSV) for manufacturing and laboratory systems. Supports HVAC, water system, and utility validation and requalification activities. Prepares validation master plans and annual product reviews related to validation. Coordinates with QA and production teams for validation scheduling and execution. Reviews equipment calibration programs and supports metrology activities. Manages validation change control and periodic review of validated systems. Prepares technical reports and deviation reports related to validation activities. Supports regulatory inspections with validation documentation and data packages. Stays updated with FDA process validation guidance, Annex 15, and ICH Q10.

Develops and implements community health programs and disease prevention initiatives. Conducts epidemiological surveillance and outbreak investigation. Manages immunization campaigns and public health interventions. Collaborates with government agencies on national health programs. Analyzes public health data for disease trends and risk factors. Designs health education and behavior change communication programs. Manages maternal and child health programs in rural and urban settings. Coordinates with ASHA workers, ANMs, and community health workers. Prepares public health reports and policy recommendations. Manages health data collection and HMIS reporting systems. Participates in disaster health preparedness and response planning. Builds partnerships with NGOs and CSOs for community health. Conducts health needs assessments and impact evaluations.

Interprets diagnostic imaging including X-rays, CT, MRI, and ultrasound. Provides timely and accurate radiology reports for clinical decision-making. Performs interventional procedures including biopsies and drainages. Collaborates with clinical teams on imaging protocol selection. Reviews imaging studies for emergency, ICU, and OPD patients. Maintains quality standards for radiology department operations. Supervises radiographers and radiology technicians daily. Participates in radiology-clinical correlation meetings. Manages PACS systems and digital image archiving. Contributes to radiology research and quality improvement projects. Stays updated with advances in AI-assisted diagnostic imaging. Ensures radiation safety protocols are strictly followed. Conducts training sessions for residents and medical students.

Position: Clinical Data Management - Trial Manager Join our forward-thinking team as a Clinical Data Management - Trial Manager and play a pivotal role in our continued success. This role provides exposure to strategic initiatives and direct collaboration with senior leadership. Role Responsibilities: Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Track milestones and coordinate with sites, CROs, and sponsors for on-time delivery. Review source data and ensure completeness, accuracy, and regulatory compliance. Develop SOPs, work instructions, and training materials for clinical operations teams. Conduct benefit-risk assessments and contribute to clinical development strategy discussions. Support IND, NDA, MAA, and dossier submissions with high-quality regulatory documentation. Plan, monitor, and close clinical trials in compliance with GCP and ICH guidelines. Develop SAS programs for SDTM/ADaM dataset creation and table, figure, listing generation. Education and Experience Requirements: Experience collaborating within cross-functional teams and matrix organisational structures. A bachelor's degree or higher in a relevant field; postgraduate qualifications are an added advantage. Proven ability to manage competing priorities in a deadline-driven, dynamic environment. Excellent verbal and written communication skills; fluency in English is essential. Demonstrated proficiency with industry-standard tools, platforms, and methodologies. High degree of professionalism, integrity, and alignment with organisational values. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. This role offers exceptional career growth, a collaborative culture, and a compensation structure aligned to market benchmarks.